chr10:89711981:T>C Detail (hg19) (PTEN)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr10:89,711,981-89,711,981
hg38	chr10:87,952,224-87,952,224 View the variant detail on this assembly version.

HGVS

PTEN

Type	Transcript	Protein
RefSeq	NM_000314.6:c.599T>C	NP_000305.3:p.Phe200Ser
	NM_001304717.2:c.599T>C	NP_001291646.2:p.Phe200Ser
	NM_001304718.1:c.599T>C	NP_001291647.1:p.Phe200Ser
Ensemble	ENST00000688308.1:c.599T>C	ENST00000688308.1:p.Phe200Ser
	ENST00000371953.8:c.599T>C	ENST00000371953.8:p.Phe200Ser
	ENST00000700029.2:c.599T>C	ENST00000700029.2:p.Phe200Ser
	ENST00000713839.1:c.692T>C	ENST00000713839.1:p.Phe231Ser
	ENST00000700021.1:c.554T>C	ENST00000700021.1:p.Phe185Ser
	ENST00000472832.3:c.599T>C	ENST00000472832.3:p.Phe200Ser

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Uncertain significance
Review star
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Links

PTEN

Type	Database	ID	Link
Gene	MIM	601728	OMIM
	HGNC	9588	HGNC
	Ensembl	ENSG00000171862	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2018-02-02	criteria provided, single submitter	not provided	germline	Detail
Uncertain significance	2020-03-23	reviewed by expert panel	PTEN hamartoma tumor syndrome	germline	Detail
Uncertain significance	2023-04-21	criteria provided, single submitter	Cowden syndrome 1	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.122	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000314.8(PTEN):c.599T>C (p.Phe200Ser) AND not provided	ClinVar	Detail
NM_000314.8(PTEN):c.599T>C (p.Phe200Ser) AND PTEN hamartoma tumor syndrome	ClinVar	Detail
NM_000314.8(PTEN):c.599T>C (p.Phe200Ser) AND Cowden syndrome 1	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs786204867 dbSNP
Genome: hg19
Position: chr10:89,711,981-89,711,981
Variant Type: snv
Reference Allele: T
Alternative Allele: C

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